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Solidea

FDA UDI

Class I (US FDA UDI)

by Calzificio Pinelli Srl

Identity

Trade Name
SOLIDEA FDA UDI
Generic Name
Compression/pressure sock/stocking, reusable FDA UDI
Device Name
WONDER MODEL 70, SIZE S, VISONE, GRADUATED COMPRESSION 12/15 mmHg SHAPEWEAR TIGHTS FDA UDI
Model / Reference
022831 FDA UDI
Description
WONDER MODEL 70, SIZE S, VISONE, GRADUATED COMPRESSION 12/15 mmHg SHAPEWEAR TIGHTS FDA UDI

Identifiers

Catalog Number
031770 FDA UDI
Primary DI / UDI-DI
08300496022831 FDA UDI
FDA Product Code
FQL FDA UDI
GMDN Term
Compression/pressure sock/stocking, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5780 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Compression/pressure sock/stocking, reusable

Solidea by Calzificio Pinelli Srl — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Compression/pressure sock/stocking, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7a5b53a5-e6a7-465b-85e1-90d1cf0e47ae 34 fields · synced May 30, 2026